Clinical Research Associate (CRA) – Maternity cover


KLIFO is looking for a Clinical Research Associate (CRA) for a one year maternity cover for our office in Glostrup

KLIFO A/S would like to engage a CRA in a one year maternity cover position. The people we want to engage like to work in a consulting environment and have a positive, proactive, flexible, self-driven and collaborative personality. We can offer a highly flexible and trustful working climate with exiting projects among competent colleagues where your contribution is valuable and makes a difference.

KLIFO is a service provider of drug development competences and operational services to the pharmaceutical, biotech and med-tech companies in Europe, US and Asia. The areas covered by KLIFO include Clinical Trial Supply Solutions, Clinical Operations Solutions, Pharmacovigilance Solutions, Regulatory Affairs Solutions, CMC Development Solutions and Drug Development Counselling.

The position as CRA:

The CRA is responsible for the pro-active site management including monitoring activity of trials, i.e.:

  • Participation in the preparation of trial documents for submissions to Competent Authorities and Ethics Committees/Institutional Review Boards
  • Visiting investigator and investigational site before a specific trial: pre-trial/site assessment visits
  • Performing initiation, monitoring and close-out visits
  • Elaboration of trial specific procedures
  • Support to data management activities
  • Continuous relationship with the Principal Investigators and trial staff to assure the success of the trial in terms of enrolment and quality
  • Assist in ensuring site compliance with protocol and trial objectives
  • Work in the clinical trial team, reporting to a project manager for trial related deliverables

The qualifications of the CRA:

The CRA should possess the following qualifications:

  • B.Sc. in the life sciences field or CRA specific diploma and a minimum of 2 years in a similar position in the pharmaceutical industry/BioTech/ CRO
  • Extensive knowledge of GCP guidelines, applicable requirements, medical terminology and clinical trial processes
  • Willingness to travel
  • Excellent verbal and communication skills
  • Excellent computer skills, ability to develop and maintain excel spreadsheets and to elaborate PowerPoint presentations
  • Strong organisational skills with attention to details

In addition to the above mentioned qualifications, the ideal candidate is a dedicated and collaborative team player, possesses excellent planning skills and is fluent spoken and written, in English and Danish.

We offer:• Work within different therapeutic areas and with tasks of varying complexity

  • Work with a heterogeneous client pool (pharmaceutical companies, established biotech, inexperienced biotech, investigators/ academia)
  • Build international client relations
  • Use – and elaborate – your competences and experience
  • Work in an interactive, flexible and positive working environment

As KLIFO is a smaller service provider, you will experience a high level of transparency, influence and a good possibility for individual planning.

Further information about KLIFO can be found at www.klifo.com

Contact:
For more information, please contact Tina Hjorth, Clinical Research Director of COS at + 45 44 222 934.

Applications should be sent to:

moc.ofilk@boj, marked ‘Clinical Research Associate‘ before 01 September 2019.

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